11 Feb 2021 - Online webinar
Also on: 23 Sep 2021
Expert advice on how to write and edit scientific and medical texts, technical documents and those documents needed for regulatory submission.
Presented by Barbara Grossman (bio)
3-4 Mar 2021 - Online webinar
Also on: 19 Oct 2021
How to produce quality regulatory documents including the clinical evaluation report (CER)
24-26 May 2021 - Online webinar
Also on: 4 Oct 2021
Success in the pharmaceutical industry depends on the speed and efficiency of new drug approvals and the quality of documentation submitted to the regulatory authorities. This intensive, practical medical writing course will benefit participants by enabling them to achieve this standard.